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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 726828Erstellt: 25. Oktober 2026

Iodine → [(S)-2-methylbutyl]phenyldichlorosilane

https://huagongshe.com/reaction/726828

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktPhenyltrichlorosilaneHCID 7372—
EduktMagnesiumHCID 5462224—
Edukt1-Bromo-2-methylbutane, (+)-HCID 5464167—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produkt[(S)-2-methylbutyl]phenyldichlorosilaneHCID 67606162—

Reaktionsschritte

Anhydrous tetrahydrofuran (125 mL) was put into a reactor with magnesium (5.7 g, 0.24 mol) and molecular sieves 4A which had been dehydrated and deaerated, followed by charging of argon gas. A small amount of iodine was slowly added to the mixture. (S)-(+)-1-bromo-2-methylbutane (30 g, 0.20 mol) was added dropwise to the slowly stirred mixture so that the reaction mixture was gradually refluxed. After the reaction was complete, the obtained Grignard reagent was transferred to a dropping funnel. The Grignard reagent was added dropwise to a solution being stirred containing phenyltrichlorosilane (50 g, 0.24 mol) in anhydrous tetrahydrofuran (50 mL) in another reactor which had been dehydrated and deaerated, followed by charging of argon gas, at 40° C.-50° C. The reaction mixture was then stirred overnight at room temperature. Hexane (500 mL) was added to the reaction mixture, and the resulting mixture was filtered under pressure, followed by fractional distillation of the filtrate to provide the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05710301
Quelldatensatzuspto-grants-1998_01
ORD IDord-68b0b1270932435b9b009a92f1bad50d
Quellennotizuspto-grants-1998_01